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地中海贫血 (简称地贫 )是遗传性珠蛋白肽链合成障碍所致的慢性溶血性贫血 ,目前药物治疗比较困难。我科于１９９８年起为１６例患者开展大部份脾栓塞术 (ＰＳＥ) ,术后经３个月至２９个月 (平均１２．６４个月 )追踪观察 ,现将临床观察报告如下。对象和方法一、对象１６例患者
Thalassemia (thalassemia) is a chronic hemolytic anemia caused by hereditary globin peptide synthesis barriers, the current drug treatment more difficult. Most of the splenic embolization (PSE) performed in 16 patients since 1998 in our department has been followed up for 3 months to 29 months (average 12.64 months). The clinical observations are as follows. Objects and methods First, the object 16 patients